Canonical Allele Identifier: CA504708536

Gene: STK11

Linked Data

• MyVariant Identifiers: chr19:g.1226544G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226545G>T , CM000681.2:g.1226545G>T	GRCh38
NC_000019.9:g.1226544G>T , CM000681.1:g.1226544G>T	GRCh37
NC_000019.8:g.1177544G>T	NCBI36
NG_007460.2:g.42139G>T , LRG_319:g.42139G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2801G>T	ENSP00000490268.2:n.*2801G>T
ENST00000585748.3:c.828G>T	ENSP00000477641.2:p.Leu276=
ENST00000585851.2:c.1026G>T	ENSP00000467912.2:p.Leu342=
ENST00000326873.12:c.1200G>T MANE Select	ENSP00000324856.6:p.Leu400=
ENST00000326873.11:c.1200G>T	ENSP00000324856.6:p.Leu400=
ENST00000585465.2:n.2933G>T
ENST00000586243.5:c.1200G>T	ENSP00000467240.2:p.Leu400=
ENST00000589152.5:n.1898G>T
NM_000455.4:c.1200G>T , LRG_319t1:c.1200G>T	NP_000446.1:p.Leu400=
XM_005259617.1:c.1195G>T	XP_005259674.1:p.Glu399Ter
XM_011528209.1:c.973G>T	XP_011526511.1:p.Glu325Ter
XM_005259617.3:c.1195G>T	XP_005259674.1:p.Glu399Ter
XM_011528209.2:c.973G>T	XP_011526511.1:p.Glu325Ter
XR_001753738.2:n.2006G>T
XR_001753740.2:n.1976G>T
NM_000455.5:c.1200G>T MANE Select	NP_000446.1:p.Leu400=